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CN100368409C - Novel 8-aza-bicyclo not 3.2.1|octane derivatives and their use as monoamine neurotransmitter re-uptake inhibitors - Google Patents

Novel 8-aza-bicyclo not 3.2.1|octane derivatives and their use as monoamine neurotransmitter re-uptake inhibitors Download PDF

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Publication number
CN100368409C
CN100368409C CNB2004800155755A CN200480015575A CN100368409C CN 100368409 C CN100368409 C CN 100368409C CN B2004800155755 A CNB2004800155755 A CN B2004800155755A CN 200480015575 A CN200480015575 A CN 200480015575A CN 100368409 C CN100368409 C CN 100368409C
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azabicyclo
octane
outward
methyl
base
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CN1798745A (en
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D·佩特斯
B·L·埃里克森
E·O·奈尔森
J·希尔-克鲁格
G·M·奥尔森
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NTG Nordic Transport Group AS
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Abstract

This invention relates to novel 8-aza-bicyclo[3.2.1]octane derivatives useful as monoamine, neurotransmitter re-uptake inhibitors. In other aspects the invention relates to the use of these compounds in a method for therapy and to pharmaceutical compositions comprising the compounds of the invention.

Description

8-azabicyclo [3.2.1] Octane derivatives and be used to prepare the purposes of monoamine neurotransmitter re-uptake
Technical field
The present invention relates to 8-aza-bicyclo [3.2.1] Octane derivatives as the novelty of monoamine neurotransmitter re-uptake.
In others, the present invention relates to the purposes of these compounds in methods of treatment and the pharmaceutical composition that comprises compound of the present invention.
Background of invention
W0/97/30997 (NeuroSearch A/S) has described has the active tropane of neurotransmitter re-uptake (tropane) derivative.
But, exist lasting intensive need find that for example serotonin reuptake transporter is to the compound of norepinephrine and Dopamine HCL activity ratio at the biological chemical performance that has optimization aspect the re-uptake activity of monoamine neurotransmitter serotonin, Dopamine HCL and norepinephrine.
Summary of the invention
In first aspect, the invention provides the compound of formula I:
Figure C20048001557500091
Or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt,
R wherein a, R bWith X as to give a definition.
In its second aspect, the invention provides a kind of pharmaceutical composition, it comprises the compound of the present invention for the treatment of significant quantity, or any its isomer, or any mixture of its isomer, or its pharmacy acceptable salt, and at least a pharmaceutically acceptable supporting agent, vehicle or thinner.
Further, the invention provides The compounds of this invention or any its isomer, or any mixture of its isomer, or its pharmacy acceptable salt is used to prepare treatment, prevent or alleviate the purposes that Mammals comprises the pharmaceutical composition of Human diseases or obstacle or illness, and described disease or obstacle or illness are replied the inhibition of monoamine neurotransmitter re-uptake in the central nervous system.
Aspect further, the present invention relates to treat, prevent or alleviate the method that animal body alive comprises Human diseases or obstacle or illness, described disease or obstacle or illness are replied the inhibition of monoamine neurotransmitter re-uptake in the central nervous system, and this method comprises the compound of the present invention of the animal body administering therapeutic significant quantity of this kind work that needs are arranged or any mixture of any its isomer or its isomer or the step of its pharmacy acceptable salt.
Those skilled in the art can obviously find out other purpose of the present invention according to the description and the embodiment of following detailed description.
Detailed Description Of The Invention
8-aza-bicyclo [3.2.1] Octane derivatives
In its first aspect, the invention provides the compound of formula I:
Or any mixture of any its isomer or its isomer,
Or its pharmacy acceptable salt,
Wherein
R aRepresent hydrogen or alkyl;
This alkyl randomly independently is selected from following substituting group and replaces by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, hydroxyl, amino, nitro, alkoxyl group, cycloalkyloxy, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl;
X representative-O-,-S-or-NR c-;
Wherein, R cRepresent hydrogen, alkyl ,-C (=O) R dOr-SO 2R d
R wherein dRepresent hydrogen or alkyl;
R bRepresent alkyl or heteroaryl,
Described aryl or heteroaryl are optional independently to be selected from following substituting group and to replace by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, hydroxyl, amino, nitro, alkoxyl group, cycloalkyloxy, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl.
In one embodiment,
R aRepresent hydrogen or alkyl;
X representative-O-,-S-or-NR c-;
Wherein, R cRepresent hydrogen, alkyl ,-C (=O) R dOr-SO 2R d
R wherein dRepresent hydrogen or alkyl;
R bRepresent alkyl or heteroaryl,
Described aryl or heteroaryl are optional independently to be selected from following substituting group and to replace by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, hydroxyl, amino, nitro, alkoxyl group, cycloalkyloxy, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl.
In further embodiment, R aRepresent hydrogen or alkyl.In embodiment further, R aRepresent hydrogen.In further embodiment, R aRepresent alkyl, as methyl.In embodiment further, R aThe alkyl that representative is replaced by hydroxyl, cyano group, cycloalkyl or alkenyl.In a concrete embodiment, R aThe representation hydroxy alkyl is as hydroxyethyl.In further embodiment, R aRepresent the cyano group alkyl, as cyano methyl.In embodiment further, R aThe representation ring alkyl alkyl is as the cyclopropyl methyl.In further embodiment, R aRepresent alkenyl alkyl, as allyl group.
In further embodiment, X representative-O-.In embodiment further, X representative-S-.In further embodiment, X representative-NR c-.In-individual concrete embodiment, R cRepresent hydrogen.In further embodiment, R cRepresentative-C (=O) R dIn a concrete embodiment, R dRepresent hydrogen.In a concrete embodiment, X representative-NH-or-N ((C=O) H)-.
In further embodiment, R bRepresent aryl or heteroaryl, this aryl or heteroaryl are optional independently to be selected from following substituting group and to replace by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, oxo and alkoxyl group.In embodiment further, R bRepresent aryl or heteroaryl, this aryl or heteroaryl are optional independently to be selected from following substituting group and to replace by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group and alkoxyl group.In further embodiment, R bRepresent aryl or heteroaryl, this aryl or heteroaryl are optional independently to be selected from following substituting group and to replace by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, oxo, alkyl and alkoxyl group.In embodiment further, R bRepresent aryl or heteroaryl, this aryl or heteroaryl are optional independently to be selected from following substituting group and to replace by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, oxo and alkoxyl group.In further embodiment, R bRepresent aryl or heteroaryl, this aryl or heteroaryl optional by one or more independently be selected from following be substituted in replace: halogen, trifluoromethyl, trifluoromethoxy, cyano group and alkoxyl group.
In further embodiment, R bRepresentative is unsubstituted, the single replacement or dibasic aryl or heteroaryl.
In embodiment further, R bThe optional substituted bicyclic heteroaryl of representative.In further embodiment, R bThe optional substituted bicyclic heteroaryl of representative.In embodiment further, R bThe optional substituted polyheteroaromatic of representative.
In a concrete embodiment, R bThe compound of optional substituted heteroaryl of representative and formula I is outer configuration.In further embodiment, R aRepresent hydrogen and R bThe optional substituted heteroaryl of representative.In embodiment further, R aRepresent hydrogen, R bThe compound of optional substituted heteroaryl of representative and formula I is outer configuration.
In embodiment further, R bThe optional substituted phenyl of representative.In further embodiment, R bThe optional substituted naphthyl of representative.In embodiment further, R bThe optional substituted fluorenyl of representative.
In further embodiment, R bThe optional substituted thienyl of representative.In embodiment further, R bThe optional substituted benzisothiazole base of representative.
In embodiment further, R bRepresent phenyl, this phenyl is optional independently to be selected from following substituting group and to replace by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group and alkoxyl group.
In further embodiment, R bRepresentative is optional by halogen such as chlorine replacement phenyl once or twice.In a concrete embodiment, R bRepresent phenyl.In further embodiment, R bRepresent mono-substituted phenyl.In a concrete embodiment, R bRepresent chloro-phenyl-, as the 3-chloro-phenyl-.In further embodiment, R bRepresent dibasic phenyl.In a concrete embodiment, R bRepresent dichlorophenyl, as 2,3-dichlorophenyl or 3,4-dichlorophenyl.In further embodiment, R bRepresentative is by the phenyl of chlorine and fluorine replacement, as 4-chloro-3-fluorophenyl or 4-fluoro-3-chloro-phenyl-.In embodiment further, R bRepresentative is by the phenyl of chlorine and trifluoromethyl replacement, as 2-chloro-3-trifluoromethyl or 4-chloro-3-trifluoromethyl.In embodiment further, R bRepresentative is by the phenyl of fluorine and trifluoromethyl replacement, as 4-fluoro-3-trifluoromethyl.In further embodiment, R bRepresentative is by the phenyl of chlorine and cyano group replacement, as 3-chloro-4-benzonitrile base.In embodiment further, R bRepresentative is by chlorine and methyl substituted phenyl, as 4-chloro-3-aminomethyl phenyl.In further embodiment, R bRepresentative is by the phenyl of chlorine and bromine replacement, as 4-bromo-3-chloro-phenyl-.In embodiment further, R bRepresent mono-substituted phenyl.In embodiment further, R bRepresent chloro-phenyl-, as 3-chloro-phenyl-or 4-chloro-phenyl-.In further embodiment, R bRepresent Trifluoromethoxyphen-l, as 3-Trifluoromethoxyphen-l or 4-Trifluoromethoxyphen-l.In embodiment further, R bRepresent trifluoromethyl, as the 4-trifluoromethyl.In further embodiment, R bThe represent methylidene phenyl is as the 4-aminomethyl phenyl.In embodiment further, R bThe representation methoxy phenyl is as 3-p-methoxy-phenyl or 4-p-methoxy-phenyl.In embodiment further, R bRepresent cyano-phenyl, as the 4-cyano-phenyl.
In further embodiment, R aRepresent hydrogen and R bRepresent phenyl, this phenyl independently is selected from following substituting group and is replaced twice: halogen, trifluoromethyl, trifluoromethoxy, cyano group and alkoxyl group.
In further embodiment, R bRepresent naphthyl, as 1-naphthyl or 2-naphthyl.In embodiment further, R bRepresentative is by halogen such as chlorine or bromine replacement naphthyl once or twice.In a concrete embodiment, R bRepresent chloronaphthyl, methylnaphthyl, as 4-chloronaphthalene-1-base.In further embodiment, R bRepresent the bromonaphthalene base, as 6-bromonaphthalene-2-base.In embodiment further, R bRepresent alkoxy such as methoxyl group replacement naphthyl once or twice.In a concrete embodiment, R bThe representation methoxy naphthyl is as 4-methoxynaphthalene-1-base, 6-methoxynaphthalene-2-base or 7-methoxynaphthalene-2-base.In embodiment further, R bRepresentative is by cyano group replacement naphthyl once or twice.In a concrete embodiment, R bRepresent the cyano group naphthyl, as 6-cyano group naphthalene-2-base.
In embodiment further, R bRepresent 1,2,3, the 4-tetralyl, as 1,2,3,4-naphthane-6-base.
In further embodiment, R bRepresent indanyl, as the 5-indanyl.
In embodiment further, R bThe fluorenyl that representative is replaced by oxo is as fluorenes-9-ketone-2-base.
In embodiment further, R bRepresent thienyl.This thienyl independently is selected from following substituting group and replaces by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group and alkoxyl group.
In further embodiment, R bRepresentative is through halogen, as chlorine or bromine replacement one or thienyl repeatedly.In a concrete embodiment, R bRepresent the bromothiophene base, as 4-bromothiophene-2-base.In further embodiment, R bRepresent the dihalo thienyl, as bromo-chloro-thienyl, especially 3-bromo-5-chloro-thiophene-2-base or 4-bromo-5-chloro-thiophene-2-base.In further embodiment, R bRepresent the dichloro-thiophene base, as 3,4-two chloro-thiophene-2-base.In also having a concrete specific examples, R bRepresent three chloro-thienyls, as 3,4,5-three chloro-thiophene-2-base.In-concrete embodiment, R bRepresent the tribromo thienyl, as 3,4,5-three bromo-thiophene-2-base.
In embodiment further, R bRepresent the benzisothiazole base, as 1,2-benzisothiazole-3-base.
In further embodiment, R bThe optional substituted benzothiazolyl of representative.In a concrete embodiment, R bRepresent benzothiazolyl, as benzothiazole-2-base.In further embodiment, R bRepresentative is by halogen such as chlorine replacement benzothiazolyl once or twice.In a concrete embodiment, R bRepresent the chloro benzo thiazolyl, as 6-chloro benzothiazole-2-base.
In further embodiment, R bRepresentative is by halogen such as bromine replacement thiazolyl once or twice.In a concrete embodiment, R bRepresent the bromethiazole base, as 5-bromo thiazole-2-base.
In embodiment further, R bRepresent quinoxalinyl, as quinoxaline-2-base.
In further embodiment, R bRepresent quinazolyl, as quinazoline-2-base.
In further embodiment, R bRepresent quinolyl, as quinoline-2-base, quinoline-6-base or quinoline-8-base.
In further embodiment, R bRepresent isoquinolyl, as isoquinoline 99.9-5-base.
In embodiment further, R bRepresent the benzoxazol base, as benzoxazol-2-base.
In further embodiment, R bThe optional substituted pyridazinyl of representative.In embodiment further, R bRepresentative is by halogen such as chlorine replacement pyridazinyl once or twice.In a concrete embodiment, R bRepresent the chloro-pyridazine base, as 6-chloro-pyridazine-3-base.
In further embodiment, R bThe optional substituted pyridyl of representative.In further embodiment, R bRepresent pyridyl, this pyridyl independently is selected from following substituting group and replaces by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, hydroxyl and alkoxyl group.In embodiment further, R bRepresentative is by halogen such as chlorine or bromine replacement pyridyl once or twice.In a concrete embodiment, R bRepresent the chloropyridine base, as 5-chloropyridine-2-base or 6-chloropyridine-2-base.In further embodiment, R bRepresentative is by bromopyridine base such as 5-bromopyridine-2 base or 6-bromopyridine-2-base.In further embodiment, R bRepresent alkoxy such as methoxy or ethoxy replacement pyridyl once or twice.In a concrete embodiment, R bThe representation methoxy pyridyl is as 6-methoxypyridine-2-base.In a concrete embodiment, R bRepresent the ethoxy pyridine base, as 6-ethoxy pyridine-2-base.In embodiment further, R bRepresentative is by trifluoromethyl replacement pyridyl once or twice.In a concrete embodiment, R bRepresent the 5-flumethiazine base, as 5-5-flumethiazine-2-base.In further embodiment, R bRepresentative is by hydroxyl replacement pyridyl once or twice.In a concrete embodiment, R bThe representation hydroxy pyridyl is as 6-pyridone-2-base.
In further embodiment, R bRepresent isoquinolyl, as isoquinolyl-1.
In further embodiment, R bThe optional substituted pyrimidyl of representative.In embodiment further, R bRepresentative is by halogen such as bromine replacement pyrimidyl once or twice.In a concrete embodiment, R bRepresent the brominated pyrimidine base, as 5-brominated pyrimidine-2-base.
In further embodiment, R bRepresent dibenzofuran group, as diphenylene-oxide-2-base.
In embodiment further, R bRepresent indyl, draw the diindyl base as 5-.
In a concrete embodiment, compound of the present invention is:
In-3-(3,4,5-three chlorothiophenes (thiophen)-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
In-2-(3,4-dichloro-thiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(1,2-benzisothiazole-3-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-bromo thiazole-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(benzisothiazole-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-chloro benzothiazole-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoxaline-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(benzoxazol-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-chloro-pyridazine-3-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-chloro-pyridine 2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(isoquinolyl-1 oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-chloropyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-bromopyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-bromopyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-bromo pyrimi piperidine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(quinazoline-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-5-flumethiazine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4,5-three smells thiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-bromothiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(3-bromo-5-chloro-thiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(4-bromo-5-chlorothiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2, the 3-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-4-fluorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-fluorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2-chloro-3-trifluoromethyl-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(fluorenes-9-ketone-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(1.2-benzisothiazole-3-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4-dichlorobenzene sulfenyl (phenylthio))-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(3, the 4-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-4-trifluoromethylphenopendant)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2-diphenylene-oxide oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(1-naphthyloxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2-naphthyloxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-4-cyano-benzene oxygen)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-methylphenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloronaphthalene-1-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(5-chloro-pyridine-2-yl)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methoxyl group phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(isoquinoline 99.9-5-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-bromo-naphthalene-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-bromo-3-chloro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-6-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-trifluoromethoxy phenoxy base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-cyano-benzene oxygen)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-8-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methylphenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-chloropyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(5-bromopyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-bromopyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(isoquinolyl-1 oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3-Trifluoromethyl phenyl ether oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-Trifluoromethyl phenyl ether oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-methoxypyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(5-5-flumethiazine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-ethoxy pyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-fluoro-3-4-trifluoromethylphenopendant)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2, the 3-dichlorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane.
Outward-3-(3, the 4-dichlorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-4-fluorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-fluorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(2-chloro-3-trifluoromethyl-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(fluorenes-9-ketone-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4-dichlorobenzene sulfenyl)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(1-naphthyloxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(2-naphthyloxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-trifluoromethyl-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-4-cyano-benzene oxygen)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(2-diphenylene-oxide oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloronaphthalene-1-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-methylphenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methoxyl group phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(7-methoxynaphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-methoxynaphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-bromo-3-chloro-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(isoquinoline 99.9-5-yl)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-bromo-naphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-methoxyl group phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-cyano-benzene oxygen)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-6-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(1,2,3,4-naphthane-6-base oxygen base)-8-methyl-8-azabicyclo [3.2,1] octane;
Outward-3-(4-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methylphenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(8-quinolyl)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-indanyl oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methoxynaphthalene-1-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(indoles-5-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-Trifluoromethyl phenyl ether oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-Trifluoromethyl phenyl ether oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-fluoro-3-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(3, the 4-dichlorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-(2-hydroxyethyl)-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-(cyano methyl)-8-azabicyclo [3.2.1] octane;
Outward-3-(3.4-dichlorophenoxy)-8-(cyclopropyl methyl)-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-(allyl group)-8-azabicyclo [3.2.1] octane;
Outward-3-(3.4-dichlorophenoxy)-8-(methoxy ethyl)-8-azabicyclo [3.2.1] octane;
Outward-3-(6-methoxypyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-ethoxy pyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-hydroxyl-pyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-cyano group-naphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4-two chloro-phenyl)-(8-methyl-8-aza-bicyclo [3.2.1] oct-3-yl)-amine;
In-(3,4-two chloro-phenyl)-(8-methyl-8-aza-bicyclo [3.2.1] oct-3-yl)-methane amide;
Outward-(3,4-two chloro-phenyl)-(8-methyl-8-aza-bicyclo [3.2.1] oct-3-yl)-methane amide;
Or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt class.
The combination of any aforesaid two or more embodiments is considered in scope of the present invention.
The substituting group definition
In the context of the present invention, halogen is represented fluorine, chlorine, bromine or iodine.
In the context of the present invention, alkyl refers to that monovalence is saturated, the straight or branched hydrocarbon chain.This hydrocarbon chain preferably comprises 1-6 carbon atom (C 1-6-alkyl), comprise amyl group, isopentyl, neo-pentyl, tert-pentyl, hexyl and isohexyl.In a preferred embodiment, alkyl represent C 1-4-alkyl comprises butyl, isobutyl-, sec-butyl and the tertiary butyl.In another embodiment preferred of the present invention, alkyl represent C 1-3-alkyl, described group can be specially methyl, ethyl, propyl group or sec.-propyl.
In the context of the present invention, alkenyl refers to comprise the carbochain of one or more pairs of keys, comprises diene, triolefin and polyenoid.In a preferred embodiment, alkenyl of the present invention comprises 2-6 carbon atom (C 2-6-alkenyl), comprise at least one two key.In a most preferred embodiment, alkenyl of the present invention is a vinyl; 1-or 2-propenyl; 1-, 2-or 3-butenyl, or 1,3-butadiene base; 1-, 2-, 3-, 4-or 5-hexenyl, or 1, the 3-hexadienyl, or 1,3,5-hexatriene base.
In the context of the present invention, alkynyl refers to comprise the carbochain of one or more three keys, comprises diine, three alkynes and polyyne.In a preferred embodiment, alkynyl of the present invention comprises 2-6 carbon atom (C 2-6-alkynyl), comprise at least one three key.In its most preferred embodiment, alkynyl of the present invention is an ethynyl; 1-or 2-propynyl; 1-, 2-or 3-butynyl, or 1,3-diacetylene base; 1-, 2-, 3-, 4-pentynyl, or 1,3-pentadiine base; 1-, 2-, 3-, 4-or 5-hexin base, or 1,3-hexadiyne base or 1,3, oneself three alkynyls of 5-.
In the context of the present invention, cycloalkyl finger ring type alkyl preferably comprises 3-7 carbon atom (C 3-7-cycloalkyl), comprise cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and suberyl.
Alkoxyl group is the O-alkyl, wherein alkyl such as above definition.
Cycloalkyloxy means the O-cycloalkyl, wherein cycloalkyl such as above definition.
Cycloalkylalkyl means above-mentioned cycloalkyl and above-mentioned alkyl, for example means the cyclopropyl methyl.
Amino is NH 2Or NH-alkyl or N-(alkyl) 2, wherein alkyl such as above definition.
In the context of the present invention, aryl is meant isocyclic aromatic nucleus system such as phenyl, naphthyl (1-naphthyl or 2-naphthyl) or fluorenyl.Term aryl also is intended to contain partially hydrogenated carbocyclic ring aromatic nucleus system, as indanyl or 1,2,3, and the 4-tetralyl.
In the context of the present invention, heteroaryl is meant aromatic monocycle or bicyclic heterocyclic radical, and it carries one or more heteroatomss in its ring texture.Preferred heteroatoms comprises nitrogen (N), oxygen (O) and sulphur (S).
That the preferred bicyclic heteroaryl of the present invention comprises is aromatic five-and hexa-member heterocycle monocycle base, and it comprises such as but not limited to  azoles base ( azoles-2-base,-4-base or-the 5-yl), different  azoles base (different  azoles-3-base,-4-base or-the 5-yl), thiazolyl (thiazol-2-yl,-4-base or-the 5-yl), isothiazolyl (isothiazole-3-base,-4-base or-the 5-yl), 1,2,4- di azoly (1,2,4- diazole-3-base or-the 5-yl), 1,2,4-thiadiazolyl group (1,2,4- diazole-3-base or-the 5-yl), 1,2,5- di azoly (1,2,5- diazole-3-base or-the 4-yl), 1,2,5-thiadiazolyl group (1,2,5-thiadiazoles-3-base or-the 4-yl), imidazolyl (2-, 4-or 5-imidazolyl), pyrryl (2-or 3-pyrryl), furyl (2-furyl, 3-furyl), thienyl (2-thienyl, the 3-thienyl), pyridyl (2-, 3-or 4-pyridyl), pyrimidyl (2-, 4-, 5-or 6-pyrimidyl), or pyridazinyl (3-or 4-pyridazinyl).
Preferred bicyclic heteroaryl of the present invention comprises the indolizine base, especially 2-, 5-or 6-indolizine base; Indyl, especially 2-, 5-or 6-indyl; Pseudoindoyl, especially 2-, 5-or 6-pseudoindoyl; Indazolyl, especially 1-or 3-indazolyl; Benzo [b] furyl, especially 2-, 5-or 6-benzofuryl; Benzo [b] thienyl, especially 2-, 5-or 6-benzothienyl; Benzimidazolyl-, especially 2-, 5-or 6-benzimidazolyl-; Benzoxazol base, especially 2-, 5-or 6-benzoxazol base; Benzothiazolyl, especially 2-, 5-or 6-benzothiazolyl; Benzisothiazole base (1,2-benzisothiazole base or 2,1-benzisothiazole base), especially 1,2-benzisothiazole-3-base; Purine radicals, especially 2-or 8-purine radicals; Quinolyl, especially 2-, 3-, 6-, 7-or 8-quinolyl; Isoquinolyl, especially 1-, 3-, 5-, 6-or 7-quinolyl; Cinnolines base, especially 6-or 7-cinnolines base; Phthalazinyl (phthalazinyl), especially 6-or 7-phthalazinyl; Quinazolyl, especially 2-, 6-or 7-quinazolyl; Quinoxalinyl, especially 2-or 6-quinoxalinyl; 1,8-naphthyridines (naphthyridinyl), especially 1,8-naphthyridines-2-, 3-, 6-or 7-base; Pteridine radicals, especially 2-, 6-, 7-pteridine radicals; And indenyl, especially 1,2-, 3-, 5-or 5-indenyl.
Preferred polyheteroaromatic of the present invention comprises dibenzofuran group, especially the 2-dibenzofuran group.
Pharmacy acceptable salt
The form that compound of the present invention can anyly be suitable for the target administration provides.Suitable form comprises pharmaceutically the salt and the prodrug forms of (being on the physiology) acceptable The compounds of this invention.
The example of pharmaceutically acceptable addition salt includes but not limited to nontoxic inorganic and organic acid addition salt, for example by hydrochloric acid deutero-hydrochloride, by Hydrogen bromide deutero-hydrobromate, by nitric acid deutero-nitrate, by perchloric acid deutero-perchlorate, by phosphoric acid deutero-phosphoric acid salt, by sulfuric acid deutero-vitriol, by formic acid deutero-formate, by acetate deutero-acetate, by equisetic acid deutero-aconitate, by xitix deutero-ascorbate salt, by Phenylsulfonic acid deutero-benzene sulfonate, by phenylformic acid deutero-benzoate, by styracin deutero-cinnamate, by citric acid deutero-Citrate trianion, by pamoic acid deutero-embonate, by enanthic acid deutero-enanthate, fumarate by fumarate derivative, by gluconic acid deutero-gluconate, by oxyacetic acid deutero-hydroxyl acetate, by lactic acid deutero-lactic acid salt, by toxilic acid deutero-maleate, by propanedioic acid deutero-malonate, by amygdalic acid deutero-mandelate, by methylsulfonic acid deutero-mesylate, by naphthalene-2-sulfonic acid deutero-naphthalene-2-sulfonic acid salt, by phthalic acid deutero-phthalate, by Whitfield's ointment deutero-salicylate, by Sorbic Acid deutero-sorbate, the stearate of deriving by stearic acid, by succsinic acid deutero-succinate, the tartrate of deriving by tartrate, by tosic acid deutero-tosilate etc.These salt can be by method preparation known in this area and that described.
Be considered to pharmaceutically unacceptable other acid and can be used to prepare the intermediate product that is used as acquisition compound of the present invention and pharmaceutically-acceptable acid addition thereof as oxalic acid.
The pharmaceutically acceptable cationic salts of The compounds of this invention includes but not limited to contain sodium, potassium, calcium, magnesium, zinc, aluminium, lithium, choline, Methionin and the ammonium salt etc. of anionic The compounds of this invention.Such cationic salts can form according to method known in the art and that described.
Within the scope of the invention, " the  salt " of nitrogenous compound also is considered to pharmacy acceptable salt.Preferably "  salt " comprises alkyl- salt, cycloalkyl- salt and cycloalkylalkyl- salt.
The example of the prodrug forms of compound of the present invention comprises the example of the prodrug of suitable material of the present invention, is included in the adorned compound of one or more reactions or deriveding group place of parent compound.Useful especially compound is an adorned compound on carboxyl, hydroxyl or amino.The example of suitable deutero-is ester or acid amides.
Compound of the present invention can solvable or insoluble form provide with pharmaceutically acceptable solvent such as water, ethanol etc.Soluble form can also comprise hydrated form, for example monohydrate, dihydrate, semihydrate, trihydrate, tetrahydrate etc.Usually, think that soluble form is equal to insoluble form for the object of the invention.
Steric isomer
Those skilled in the art will recognize that compound of the present invention can comprise one or more chiral centres, and this compound exists with isomeric forms.
And, at substituting group-X-R of 3 of the 8-of formula I aza-bicyclo [3.2.1] octane skeleton bCan be specially outer or interior configuration.In an embodiment preferred of the present invention, 3 substituting group is outer configuration.In another embodiment preferred of the present invention, 3 substituting group is interior configuration.
The present invention includes all these isomer and any its mixture, comprise racemic mixture.
Racemic form can split into optical antipode with known method and technology.A kind of method of separating isomerism salt is to use optical activity acid, and by discharge the optical activity amine compound with alkaline purification.The another kind of method that racemic modification is split into optical antipode is handled based on the enterprising circumstances in which people get things ready for a trip spectrum of optical activity matrix.Therefore for example can split into their optical antipode by fractional crystallization d-or 1-(tartrate, mandelate or camsilate) and with racemic compound of the present invention.
Compound of the present invention can also split by the following method: make compound of the present invention and optical activity activatory carboxylic acid as forming the diastereomer acid amides by (+) or (-) phenylalanine, (+) or (-) phenylglycocoll, (+) or (-) dextrocamphoric acid deutero-carboxylic acid reaction, perhaps make reactions such as compound of the present invention and optical activity chloro-formic ester form the diastereomer carbamate.
Other method that is used to split optical isomer is well known in the art.These methods comprise Jaques J, ColletA ， ﹠amp; Wilen S in " Enantiomers.Racemates, andResolutions ", John Wiley and Sons, the described method of New York (1981).
Optically active compound can also be by the optical activity feedstock production.
Tagged compound
Compound of the present invention can their mark or unlabelled form use.Within the scope of the present invention, " mark " representative is bonded to compound of interest with marker, thereby makes the detection by quantitative of this compound easy.
The compound of mark of the present invention can be used as diagnostic tool, radiotracer or the monitoring agent in the multiple diagnostic method, and is used for the imaging of body inner recipient.
The isomer of mark of the present invention preferably comprises at least one radionuclide and serves as a mark.The radionuclide of emission positron is all purposes material standed fors.Within the scope of the invention, radionuclide is preferably selected from 2H (deuterium), 3H (tritium), 13C, 14C, 131I, 125I, 123I and 18F.
The physical method that is used to detect the isomer of mark of the present invention can be selected from PET (positron emission tomography) (PET), single photon tomography computer fault imaging (SPECT), nuclear magnetic resonance spectroscopy (MRS), nuclear magnetic resonance (MRI) and axial X-ray topography of area of computer aided (CAT) or their combination.
The preparation method
Compound of the present invention can be by being used for the ordinary method of chemosynthesis, for example described in an embodiment method preparation.The raw material that is used for the described method of the application is known, perhaps can easily be prepared by the chemical substance that is available commercially by ordinary method.
Can also change into another kind of compound of the present invention with ordinary method a kind of compound of the present invention.
The end product of reaction as herein described can pass through routine techniques, for example waits by extraction, crystallization, distillation, chromatography and separates.
Biological activity
Can test compound of the present invention and suppress the ability of the re-uptake of monoamine Dopamine HCL, norepinephrine and serotonin in the synaptosome, as described in the WO97/30997.According to observed equilibrium activity in these tests, consideration with compound of the present invention be used for the treatment of, prevention or releasing mammal, the disease that comprises the people or obstacle or illness, described disease, obstacle or illness are replied the inhibition of the monoamine neurotransmitter re-uptake in the central nervous system.
In a specific embodiment, consider compound of the present invention is used for the treatment of, prevention or alleviation: emotional handicap, depressed, the atypia depression, major depressive disorder, evil mood, bipolar disorder, I type bipolar disorder, II type bipolar disorder, the cyclothymia obstacle, the emotional handicap that causes by the general medicine illness, material inductive emotional handicap, pseudodementia, Ganser's syndrome, obsessional idea and behavior disorder, Phobias, the Phobias of no agoraphobia, the Phobias that agoraphobia is arranged, the agoraphobia of no Phobias medical history, panic attack, memory impairment, the loss of memory, attention deficit hyperactivity disease, fat, anxiety, generalized anxiety disorder, eating disorder, Parkinson's disease, the Parkinson dementia, the aging dementia, senile dementia, Alzheimer, the dull-witted complex of acquired immune deficiency syndrome (AIDS), aging memory machine dysfunction, specific phobia disease, social phobia, nervous obstacle after the wound, acute nervous obstacle, drug habit, drug abuse, cocaine abuse, the nicotine abuse, tobacco abuse, alcohol addiction, alcoholism, pain, chronic pain, inflammatory pain, neuropathic pain, migraine, tension-type headache, chronic tension-type headache, the pain relevant with depression, fibromyalgia, sacroiliitis, osteoarthritis, rheumatoid arthritis, back pain, cancer pain, intestines easily swash property pain, irritable bowel syndrome, post-operative pain, pain after the apoplexy, drug-induced neuropathy, diabetic neuropathy, sympathetic nerve maintenance pain, trigeminal neuralgia, toothache, muscular fascia pain, phantom limb pain, exessive appetite, syndrome before the menstruation, the evening luteal phase syndrome, posttraumatic syndrome, chronic fatigue syndrome, the urinary incontinence, stress incontinence, urge incontinence, night the urinary incontinence, sexual dysfunction, premature ejaculation, it is difficult to erect, erection problem, eating disorder, anorexia nervosa, somnopathy, autism, mutism, trichotillomania, hypnolepsy, the apoplexy retarded depression, apoplexy inductive brain injury, apoplexy inductive neuronal damage or Du Leite disease.In a preferred embodiment, consideration with this compound be used for the treatment of, prevention or alleviate depression.
The suitable dosage range of considering active pharmaceutical ingredient (API) at present is about 0.1 to about 1000mg API/ day, more preferably about 10 to about 500mg API/ days, most preferably about 30 to about 100mg API/ days, but depend on the indication of definite administering mode, form of medication, consideration, experimenter, particularly related experimenter's body weight and preference and the experience of further being responsible for physician or animal doctor.
Preferred compound of the present invention is in sub-micro mole and micro-molar range, promptly demonstrate biological activity less than 1 to about 100 μ M.
Pharmaceutical composition
On the other hand, the invention provides the new pharmaceutical composition that comprises the compound of the present invention for the treatment of significant quantity.
Though the form administration that the compound of the present invention that is used for the treatment of can original chemical, preferred activeconstituents and one or more auxiliary agents, vehicle, carrier, buffer reagent, thinner and/or other conventional medicine auxiliary agent of in pharmaceutical composition, introducing optional for acceptable salt form on the physiology.
Therefore in a preferred embodiment, the invention provides and comprise The compounds of this invention or its pharmaceutically acceptable derivates, with one or more pharmaceutically acceptable carriers, and in optional this area known and use other treat and/or prevent composition pharmaceutical composition.This carrier must be that the implication of " acceptable " is compatible with other composition of preparation, and harmless to its receptor.
Pharmaceutical composition of the present invention can be the pharmaceutical composition that is suitable for mouth, rectum, segmental bronchus, nose, lung, part (comprising cheek and hypogloeeis), transdermal, vagina or parenteral (comprise in skin, subcutaneous, intramuscular, intraperitoneal, intravenously, intra-arterial, the brain, intraocular injection or infusion) administration, or be suitable for by sucking or be blown into administration, comprise powder or liquid aersol administration, or pass through the form of sustained release system administration.The example of suitable sustained release system comprises the semipermeability matrix of the solid hydrophobic polymkeric substance that comprises The compounds of this invention, and described matrix can be the form of shaped particles, for example film or micro-capsule.
Compound of the present invention can be put into the formulation of pharmaceutical composition or its dosage unit with auxiliary agent, carrier or the thinner of routine.These formulations comprise solid, particularly tablet, filled capsules, powder and pill, and the capsule (they all are used for oral) of liquid, the particularly aqueous solution or non-aqueous solution, suspension, emulsion, elixir and this compound of filling, be used for the suppository of rectal administration and be used for the aseptic injectable solution of parenteral applications.This pharmaceutical composition and unit dosage form thereof can comprise the conventional ingredient of conventional ratio, and contain or do not contain additional active compound or composition, and this unit dosage form can comprise any suitable suitable effective amount of actives of using with expectation of per daily dose scope.
Compound of the present invention can multiple oral and parenteral dosage forms administration.Those skilled in the art obviously following as can be seen formulation can comprise the pharmacy acceptable salt of compound of the present invention or The compounds of this invention as activeconstituents.
For by compound pharmaceutical composition of the present invention, pharmaceutically acceptable carrier can be solid or liquid.But solid preparation comprises powder, tablet, pill, capsule, lozenge, suppository or discrete particles.Solid carrier can be one or more materials that can also be used as thinner, seasonings, stablizer, lubricant, suspending agent, tackiness agent, sanitas, tablet disintegrant or encapsulated materials.
In powder, carrier can be the solid of segmentation, and it mixes with the activeconstituents that segments.
In tablet, activeconstituents mixes with an amount of carrier with necessary adhesive capacity, and is pressed into target shape and size.
Powder and tablet preferably comprise 5 or 10% to about 70% active compound.Suitable carrier is magnesiumcarbonate, Magnesium Stearate, talcum, sugar, lactose, pectin, dextrin, starch, gelatin, tragacanth gum, methylcellulose gum, Xylo-Mucine, low melt wax, cocoa wet goods.Terms " formulation " means and comprises and contain encapsulated materials as the preparation of the active compound of capsular carrier is provided, and wherein surrounds with carrier and contains or not carrier-containing described activeconstituents, thereby make its combination.Similarly, the present invention includes lozenge and sugar shallow lake.Tablet, powder, capsule, pill, lozenge and sugared shallow lake can be as being suitable for oral solid dosage.
For preparation suppository, at first with low melt wax, the mixture melt of fatty acid glycerine or theobroma oil for example, and by stirring active ingredient is scattered in wherein equably.With the conventional big or small mould of the uniform mixture impouring of fusing, make its cooling, thereby make its curing then.
The composition that is suitable for vagina administration can provide with the form of the hysterophore, cotton balls, emulsifiable paste, gel, paste, foam or the sprays that comprise activeconstituents and appropriate carrier as known in the art.
Liquid preparation comprises solution, suspension and emulsion, for example water or water-propylene glycol solution.For example, the parenteral injection liquid preparation can be formed in the solution in the polyoxyethylene glycol aqueous solution.
Therefore, compound of the present invention be used for administered parenterally (for example by injection, as bolus injection or connect inculcate), and can inculcate or the unit dosage form of multi-dose container provides at ampoule, pre-filled syringe, the small volume that contains the sanitas of adding.Said composition can be the form of suppository, solution or the emulsion in oil or vehicle, and can comprise preparation reagent such as suspending agent, stablizer and/or dispersion agent.As alternative selection, activeconstituents can obtain by aseptic separation sterile solid or by freeze-drying solution by powder type, is used for before use and suitable vehicle such as aseptic, as not contain pyrogen water preparation.
The aqueous solution that is suitable for mouthful usefulness can be by water-soluble with activeconstituents, and add suitable tinting material, seasonings, stablizer and thickening material and prepare.
The aqeous suspension that is suitable for mouthful usefulness can be dissolved in the water that contains viscous substance by the active ingredient with segmentation, and for example natural or synthetic gum, resin, methylcellulose gum, Xylo-Mucine or other known suspending agent prepare.
The present invention also comprises and changes into the solid dosage that is used for oral liquid preparation in the short period of time before being intended to use.These liquid dosage forms comprise solution, suspension and emulsion.Except active ingredient, these preparations can comprise tinting material, seasonings, stablizer, buffer reagent, artificial and synthetic sweetener, divide powder, thickening material, solubility promoter etc.
For epidermis is carried out topical, compound of the present invention can be made ointment, emulsifiable paste or washing lotion, perhaps make transdermal patch.For example, ointment and emulsifiable paste can use or oleaginous bases, and add suitable thickening and/or gelling reagent and prepare.Washing lotion can use or the oleaginous base preparation, and generally also comprises one or more emulsifying agents, stablizer, dispersion agent, suspending agent, thickening material or tinting material.
Being suitable for carrying out in the oral cavity topical drug delivery composition comprises and contains at flavoured base, is generally the lozenge of the active agent in sucrose and gum arabic or the tragacanth; Be included in the lozenge (pastilles) of the activeconstituents in inert base such as gel and glycerine or sucrose and the gum arabic; With the mouthwash that is included in the activeconstituents in the appropriate liquid carrier.
By ordinary method, for example solution or suspension are directly applied to nasal cavity with dropper, suction pipe or spraying.Described composition can be single or the multiple doses form provide.
Respiratory tract administration can also be finished by the gaseous solvents preparation, wherein containing suitable propellent, for example providing in the pressure packing of Chlorofluorocarbons (CFC) as Refrigerant 12, trichlorofluoromethane or dichloro tetrafluoro ethane, carbonic acid gas or other suitable gas.Described aerosol can also comprise tensio-active agent, for example Yelkin TTS expediently.The dosage of medicine can be controlled by metering valve is provided.
As alternative selection, activeconstituents can anhydrous powder, and for example the form at the powdered mixture of suitable powder matrix such as the compound in lactose, starch, starch derivative such as Vltra tears and the polyvinylpyrrolidone (PVP) provides.Conventional powder carrier will form gel in nasal cavity.This powder composition can provide by unit dosage form, for example in gelatine capsule or cartridge case, perhaps can use in the Blister Package of powder by sucker.
Composition desiring to be used for to respiratory tract administration comprises in the intranasal compositions that this compound generally has small particle size, and for example the particle diameter order of magnitude is 5 microns or littler.This particle diameter can obtain by method as known in the art, for example obtains by micronization.
If necessary, can use the composition that is suitable for continuing release of active ingredients.
This pharmaceutical preparation is preferably unit dosage form.In this formulation, preparation is subdivided into the dosage unit that comprises an amount of active ingredient.Unit dosage form can packaged preparation, and this packing comprises the packing of the preparation of separation number amount, for example Bao Zhuan tablet, capsule and the powder in bottle or ampoule.And unit dosage form can be capsule, tablet, cachet or a lozenge itself, and perhaps it can be any of these packaged form of suitable number.
Be used for oral tablet or capsule and be used for intravenous administration and the liquid of continuous infusion is preferred compositions.
Further details about preparation and medicine-feeding technology can see Remington ' s Pharmaceutical Sciences(Maack Publishing Co., Easton, latest edition PA).
The treatment effective dose refers to alleviate the quantity of the activeconstituents of illness or illness.Treatment is renderd a service and toxicity, for example ED 50And LD 50Can determine by the cell culture or the laboratory animal pharmacological method of standard.Dosage ratio between result of treatment and the toxic action is a therapeutic index, and it can use ratio LD 50/ ED 50Expression.The big treatment of preferred performance exponential pharmaceutical composition.
Dosage must be adjusted carefully according to the result who treats individual age, weight and illness and route of administration, formulation and scheme and expectation certainly, and definite dosage should be determined by practitioner.
Actual dosage depends on the character and the severity of the disease of being treated, and in physician's judgement scope, and can change according to the titration dosage to particular case of the present invention, to produce the goal treatment effect.But, to think at present to comprise about activeconstituents of 0.1 to about 500mg/single dosage, preferably approximately 1 is to about 100mg, and most preferably about pharmaceutical composition of 1 to about 10mg is suitable for treating.
Activeconstituents can every day one or several dosed administration.In some cases, can under the dosage that is low to moderate 0.1 μ g/kgi.v. and 1 μ g/kgp.o, obtain satisfied result.Be limited to about 10mg/kgi.v. and 100mg/kg p.o on the current dose scope.Preferred range is extremely approximately 10mg/kg/ days i.v. of about 0.1 μ g/kg, and about 1 μ g/kg is to about 100mg/kg/ days p.o.
Methods of treatment
On the other hand, the invention provides and a kind ofly be used for the treatment of, prevent or alleviate moving object, comprise people's the disease or the method for obstacle or illness, described disease, obstacle or illness are replied the inhibition of the monoamine neurotransmitter re-uptake in the central nervous system, and described method comprises to the moving object that these needs are arranged, comprises that the people uses the compound of the present invention of significant quantity.
Think at present, the appropriate dosage scope is the 0.1-1000 mg/day, the 10-500 mg/day, 30-100 mg/day particularly, usually depend on definite administering mode, form of administration, administration at indication, the experimenter who relates to, the experimenter's that relates to body weight, and preference and the experience of further being responsible for physician or animal doctor.
Embodiment
Further with reference to the present invention of following examples illustration, described embodiment is not intended to the scope of the present invention that requires patent protection that limits by any way.
Universal method: all reactions that relate to the reagent of air-sensitive or intermediate all are to carry out under nitrogen and in anhydrous solvent.In reclaimer (workup-procedures), use sal epsom as siccative and vapourisation under reduced pressure solvent.
Method A
In-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
With tetrachlorothiophene (5.48 grams, 24.69 tropine (interior-the 8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) (3.48 grams mmole),, 24.69 potassium tert.-butoxide (4.16 grams mmole),, 37.04 mmole), 18-hat-6-ether (6.53 grams, 24.69 mmoles) and the mixture of DMF (50 milliliters) stirred 15 hours at 100 ℃.With aqueous hydrochloric acid (50 milliliters 4M) are added in this mixture.Wash this mixture with ether (2 * 100 milliliters).The interpolation aqueous sodium hydroxide solution (100 milliliters, 4M).With ethyl acetate (3 * 100 milliliters) this mixture is extracted.With sodium chloride aqueous solution (3 * 50 milliliters) washing organic phase.Output is 2.65 grams (33%).Obtain corresponding salt by adding with fumaric acid saturated ether and carbinol mixture (9: 1).Mp200.4-206.4℃。
In-3-(3,4-dichloro-thiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane
Be according to method A from 2,3,4-three chlorothiophenes and tropine (interior-the 8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation, with free alkali and oil form be separated.
Outward-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane hydrochloride
According to method A from tetrachlorothiophene and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp249-250℃。
Outward-3-(1,2-benzisothiazole-3-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane hydrochloride
Be according to method A from 3-chloro-1,2-benzisothiazole and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp259.4-261.2℃。
Outward-3-(5-bromo thiazole-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane
Be according to method A from 2,5-two bromo thiazoles and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Form with free alkali is separated.Mp104-106℃。
Outward-3-(benzothiazole-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
According to method A from 2-chloro benzothiazole and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp160-162℃。
Outward-3-(6-chloro benzothiazole-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be according to method A from 2,6-dichlorobenzothiazole and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp163-164.5℃。
Outward-3-quinoxaline-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
According to method A from 2-chloro-quinoxaline and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp208-210℃。
Outward-3-(quinoline-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
According to method A from 2-chloroquinoline and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp192.5-195℃。
Outward-3-(benzoxazol-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
According to method A from 2-chlorine benzoxazol and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp141-144℃。
Outward-3-(6-chlorine pyridazine-3-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be according to method A from 3,6-dichloro-pyridazine and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp181-183℃。
Outward-3-(5-chloro-pyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be according to method A from 2,5-dichloropyridine and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp214-216℃。
Outward-3-(isoquinolyl-1 oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
According to method A from 1-chlorine isoquinoline 99.9 and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp180-181.5℃。
Outward-3-(6-chloropyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be according to method A from 2,6-dichloropyridine and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp202-204℃。
Outward-3-(5-bromopyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be according to method A from 2,5-dibromo pyridine and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp213-215℃。
Outward-3-(6-bromopyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be according to method A from 2,6-dibromo pyridine and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp198-200℃。
Outward-3-(5-bromo pyrimi piperidine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
According to method A from 5-bromo-2-chloropyrimide and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp198-200℃。
Outward-3-(quinazoline-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
According to method A from 2-chloro-quinazoline and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp209-211℃。
Outward-3-(5-5-flumethiazine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
According to method A from 2-chloro-5-5-flumethiazine and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp190-191.5℃。
Outward-3-(3,4,5-three bromothiophenes-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane hydrochloride
According to method A from tetrabromothiophene and pseudotropine (outside-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp223.3-223.9℃。
Outward-3-(4-bromothiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane hydrochloride
Be from outside-3-(3,4,5-three bromothiophenes-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane by with 5 normal zinc powders in dense acetic acid in 75 ℃ stir 15 hours prepared.Finishing sequence is carried out according to method A.Mp222.1℃。
In-3-(3-bromo-5-chloro-thiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be according to method A from 3-bromo-2,5-dichloro-thiophene and tropine (interior-the 8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp171-173℃。
In-3-(4-bromo-5-chloro-thiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be according to method A from 3-bromo-2,5-dichloro-thiophene and tropine (interior-the 8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp136-139℃。
Method B
In-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane
Interior-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane (0.50 gram, 1.53 mmoles), chloroformate-1-chloro-ethyl ester (1.27 milliliters, 11.5 mmoles) and toluene (20 milliliters) backflow were stirred 15 hours.Interpolation water (10 milliliters) also stirred 3.5 hours under refluxing.Mixture is evaporated.Add sodium methylate (5 milliliters 1M) are also followed evaporation with silica gel 60 (2 gram) in the methyl alcohol.Rough mixture is carried out stratographic analysis with methylene dichloride, methyl alcohol and strong aqua (89: 10: 1) obtain to be free alkali and buttery title compound on silica gel with quantitative productive rate.
Outward-3-(2, the 3-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane
Prepare according to method B.Separate and be free alkali.Mp62.3-65.4℃。
Outward-3-(3, the 4-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane hydrochloride
Prepare according to method B.Mp160.1℃。
Outward-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane hydrochloride
Prepare according to method B.Mp255-256℃。
Outward-3-(3-chloro-4-fluoro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp151-154℃。
Outward-3-(3-chloro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp195-196℃。
Outward-3-(4-chloro-3-fluorophenoxy)-8-H-8-azabicyclo [3.2.1] octane prepares according to method B.Separate and be free alkali and oily.
Outward-3-(4-chloro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp188-188.5℃。
Outward-3-(2-chloro-3-trifluoromethyl-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp190-193℃。
Outward-3-(fluorenes-9-ketone-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane prepares according to method B.Separate and be free alkali.Mp242.8-256.3℃。
Outward-3-(1.2-benzisothiazole-3-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane hydrochloride
Be according to method B from 3-chloro-1,2-benzisothiazole and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp252.5℃。
Outward-3-(3,4-dichlorobenzene sulfenyl)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp194-196℃。
Interior-3-(3, the 4-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane hydrochloride prepares according to method B.Mp287℃。
Outward-3-(4-chloro-3-4-trifluoromethylphenopendant)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.MP215-217℃。
Outward-3-(2-diphenylene-oxide oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.MP217-221℃。
Outward-3-(1-naphthyloxy)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp223-224℃。
Outward-3-(2-naphthyloxy)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp202-204℃。
Outward-3-(3-chloro-4-cyano-benzene oxygen)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp176.3-178.9℃。
Outward-3-(4-chloro-3-methylphenoxy)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp192.5-194.5℃。
Outward-3-(4-chloronaphthalene-1-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp226-227℃。
Outward-3-(quinoline-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp211-213℃。
Outward-3-(5-chloro-pyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp196-198℃。
Outward-3-(4-methoxyl group phenoxy group)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp137-147℃。
Outward-3-(isoquinoline 99.9-5-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane trans-succinate salt
Prepare according to method B.Mp192-194℃。
Outward-3-(6-bromo-naphthalene-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane hydrochloride prepares according to method B.Separate and be free alkali.Mp270-274℃。
Outward-3-(4-bromo-3-chloro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp207-209℃。
Outward-3-(quinoline-6-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp237-239℃。
Outward-3-(4-trifluoromethoxy phenoxy base)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp178-180℃。
Outward-3-(4-cyano-benzene oxygen)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp188.9-191.6℃。
Outward-3-(quinoline-8-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp182-184.5℃。
Outward-3-(4-methylphenoxy)-8-H-8-azabicyclo [3.2.1] octane fumarate prepares according to method B.Mp174-177℃。
Outward-3-(6-chloropyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate
Be according to method B from 2,6-dichloropyridine and pseudotropine (outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) preparation.Mp202-204℃。
Outward-3-(5-bromopyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp216-218℃。
Outward-3-(6-bromopyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp218-220℃。
Outward-3-(isoquinolyl-1 oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate
Be from 1-chlorine isoquinoline 99.9 and pseudotropine (outside-8-methyl-8-azabicyclo [3,2,1] suffering-3-alcohol) preparation according to method B.Mp215-217℃。
Outward-3-(3-Trifluoromethyl phenyl ether oxygen base)-8-H-8-azabicyclo [3.2.1] octane prepares according to method B.Separate and be free alkali.Mp185.5-187℃。
Outward-3-(4-Trifluoromethyl phenyl ether oxygen base)-8-H-8-azabicyclo [3.2.1] octane prepares according to method B.Separate and be free alkali.Mp192.5-194℃。
Outward-3-(6-methoxypyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp200-202℃。
Outward-3-(5-5-flumethiazine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp196.5-198.5℃。
Outward-3-(6-ethoxy pyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp192.5-194.5℃。
Outward-3-(4-fluoro-3-4-trifluoromethylphenopendant)-8-H-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method B.Mp182-185℃。
Method C
Outward-3-(2, the 3-dichlorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
At room temperature with (8.36 milliliters of diethylazodicarboxylates, 53.1 mmole) be added drop-wise to tropine (interior-the 8-methyl-8-azabicyclo [3.2.1] suffering-3-alcohol) (5.0 grams, 35.4 mmole), 2,3-chlorophenesic acid (6.93 grams, 4 2.5 mmoles), in the mixture of triphenylphosphine (13.9 grams, 53.1 mmoles) and two  alkane (55 milliliters).Mixture was stirred 40 hours at 100 ℃.With aqueous sodium hydroxide solution (100 milliliters 1M) are added in the mixture.With methylene dichloride (2 * 100 milliliters) mixture is extracted.On silica gel, carry out stratographic analysis and produce title compound with methyl alcohol, methylene dichloride and acetone (1: 4: 1).Output is 6.22 grams (61%).Corresponding salt obtains by adding with fumaric acid saturated ether and carbinol mixture (9: 1).Mp171.3-194.7℃。
Outward-3-(3, the 4-dichlorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp225.6℃。
Outward-3-(3-chloro-4-fluorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane prepares according to method C.Separate and be free alkali and oily.
Outward-3-(4-chloro-3-fluorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane prepares according to method C.Separate and be free alkali and oily.
Outward-3-(2-chloro-3-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane prepares according to method C.Separate and be free alkali and oily.
Outward-3-(3-chloro-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane oxalate prepares according to method C.Mp208-209℃。
Outward-3-(4-chloro-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane oxalate prepares according to method C.Mp150.5-154.0℃。
Outward-3-(fluorenes-9-ketone-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane hydrochloride
Prepare according to method C.Mp decomposes.
Outward-3-(3,4-dichlorobenzene sulfenyl)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be according to method C from 3,4-thiophenol dichlorobenzene preparation.Mp179-181℃。
Outward-3-(1-naphthyloxy)-8-methyl-8-azabicyclo [3.2.1] octane
Prepare according to method C.Separate and be free alkali.Mp72-74℃。
Outward-3-(2-phenoxy group)-8-methyl-8-pyridine dicyclo [3.2.1] octane
Prepare according to method C.Separate and be free alkali.Mp83-86℃。
Outward-3-(4-chloro-3-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane fumarate.
Prepare according to method C.Mp172.3-174.2℃。
Outward-3-(3-chloro-4-cyano-benzene oxygen)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp191.7-194.3℃。
Outward-3-(2-diphenylene-oxide oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp199.9-202.0℃。
Outward-3-(4-chloronaphthalene-1-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp198-199℃。
Outward-3-(4-chloro-3-methylphenoxy)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp230-232℃。
Outward-3-(4-methoxyl group phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp164.5-166.5℃。
Outward-3-(7-methoxy naphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp143-145℃。
Outward-3-(6-methoxy naphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp78.5-81.5℃。
Outward-3-(4-bromo-3-chloro-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp218-220℃。
Outward-3-(isoquinoline 99.9-5-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp193-196℃。
Outward-3-(6-bromo-naphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp227-229℃。
Outward-3-(3-methoxy phenoxy)-8-methyl-8-azabicyclo [3.2.1] octane fumarate prepares according to method C.Mp144-147℃。
Outward-3-(4-cyano-benzene oxygen)-8-methyl-8-azabicyclo [3.2.1] octane fumarate prepares according to method C.Mp177.9-181.9℃。
Outward-3-(quinoline-6-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate prepares according to method C.Mp221-223℃。
Outward-3-(1,2,3,4-naphthane-6-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp165.9-167.2℃。
Outward-3-(4-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp184.1-186.5℃。
Outward-3-(4-methylphenoxy)-8-methyl-8-azabicyclo [3.2.1] octane fumarate prepares according to method C.Mp178-181℃。
Outward-3-(8-quinolyl oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate prepares according to method C.Mp158-160℃。
Outward-3-(5-indane oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate prepares according to method C.Mp184.7-185.9℃。
Outward-3-(4-methoxy naphthalene-1-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp185-188℃。
Outward-3-(indoles-5-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate prepares according to method C.Mp176.3-178.3℃。
Outward-3-(3-Trifluoromethyl phenyl ether oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane prepares according to method C.Separate and be free alkali.Oil.
Outward-3-(4-Trifluoromethyl phenyl ether oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane prepares according to method C.Separate and be free alkali.Oil
Outward-3-(4-fluoro-3-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method C.Mp167-169℃。
Method D
In-3-(3, the 4-dichlorophenoxy)-8-methyl-8-azabicyclo [3.2,1] octane fumarate
With interior-3-chloro-8-methyl-8-azabicyclo [3.2.1] octane (3.9 grams, 24 mmoles), (by the pure and mild thionyl chloride backflow of outer-8-methyl-8-azabicyclo [3.2.1] suffering-3-preparation in 3 hours), 3,4-chlorophenesic acid (5.9 grams, 36 mmoles), sodium hydroxide 6 0% (1.2 grams, 36 mmoles) and ethanol (30 milliliters) reflux and stirred 15 hours.Aqueous hydrochloric acid (50 milliliters 4M) are added in this mixture.Ethanol evaporation.Mixture is washed with ether (3 * 50 milliliters).The interpolation aqueous sodium hydroxide solution (50 milliliters, 4M).With ether (3 * 50 milliliters) this mixture is extracted.Rough mixture is carried out stratographic analysis with methylene dichloride, methyl alcohol and strong aqua (89: 10: 1) obtain title compound on silica gel.Obtain its corresponding salt by adding with fumaric acid saturated ether and carbinol mixture (9: 1).Output 0.90 gram (9%).Mp198.0-207.7℃。
Method E
Outward-3-(3, the 4-dichlorophenoxy)-8-(2-hydroxyethyl)-8-azabicyclo [3.2.1] octane
Will outer-3-(3, the 4-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane (2.2 grams, 8.1 mmoles), the stirring 15 hours that refluxes of ethylene bromohyrin (0.6 milliliter, 8.9 mmoles), salt of wormwood (1.1 grams, 8.1 mmoles) and ethanol (20 milliliters).The interpolation aqueous sodium hydroxide solution (50 milliliters, 4M).With methylene dichloride (3 * 50 milliliters) this mixture is extracted.Rough mixture is carried out the stratographic analysis generation with methylene dichloride, methyl alcohol and strong aqua (89: 10: 1) be free alkali and buttery title compound on silica gel.Output 0.40 gram (16%).
Outward-3-(3, the 4-dichlorophenoxy)-8-(cyanogen methyl)-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method E.Mp79-82℃。
Outward-3-(3, the 4-dichlorophenoxy)-8-(cyclopropyl methyl)-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method E.Mp187-189.5℃。
Outward-3-(3, the 4-dichlorophenoxy)-8-(allyl group)-8-azabicyclo [3.2.1] octane fumarate
Prepare according to method E.Mp202-206℃。
Outward-3-(3, the 4-dichlorophenoxy)-8-(methoxy ethyl)-8-azabicyclo [3.2.1] octane fumaric acid
Prepare according to method E.Mp177.8-179.5℃。
Method F
Outward-3-(6-methoxypyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Will outer-3-(6-chloropyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane (6.5 grams, 25.8 mmoles), the mixture of sodium methylate (6.5 grams, 0.12 mole) and NMP (30 milliliters) is 130 ℃ of stirrings 15 hours.Add water (300 milliliters).With ether (3 * 150 milliliters) this mixture is extracted.Obtain corresponding salt by adding with fumaric acid saturated ether and methyl alcohol (9: 1) mixture.Output 3.0 grams (32%).Mp176-177.5℃。
Outward-3-(6-ethoxy pyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
According to method F preparation, Mp177-179 ℃.
Outward-3-(6-hydroxyl-pyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
Be from outside-3-(6-(suitable-ethylene methacrylic oxygen base)-pyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane made by stirring under refluxing with concentrated hydrochloric acid in 0.5 hour.Aftertreatment is carried out according to method F.Mp196.5-200℃。
Method G
Outward-3-(6-cyano group-naphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane fumarate
With outer-3-(6-bromo-naphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane (2.6 grams, 7.5 mmoles), Zn (CN) 2The mixture of (2.2 grams, 18 mmoles), palladium ring (palladacycle) (50 milligrams) and two  alkane (30 milliliters) stirred 70 hours under refluxing.Aqueous sodium hydroxide solution (50 milliliters 1M) are added in this mixture.With methylene dichloride (2 * 50 milliliters) this mixture is extracted.On silica gel, carry out stratographic analysis and obtain title compound with methyl alcohol, methylene dichloride and strong aqua (1: 9: 1%).Output 2.06 grams (94%).Obtain corresponding salt by adding with fumaric acid saturated ether and carbinol mixture (9: 1).Mp230-232℃。
Method H
Outward-(3,4-two chloro-phenyl)-8-(methyl-8-aza-bicyclo [3.2.1] oct-3-yl)-amine fumarate
0 ℃ of preparation 3,4-dichloromethane anilide (0.6 gram, 3.17 tropine methanesulfonates tosylate (1.24 grams mmole),, 3.17 [people such as S.Archer mmole), JACS 80,4677-4691 page or leaf (1958)], the mixture of sodium hydride (0.17 gram, 6.97 mmoles) and DMF (5 milliliters).Mixture was at room temperature stirred 15 hours.Aqueous sodium hydroxide solution (5 milliliters 1M) are added in this mixture.With methylene dichloride (2 * 5 milliliters) this mixture is extracted.On silica gel, carry out the compound that stratographic analysis produces title with methyl alcohol, methylene dichloride and ammoniacal liquor (10: 89: 1).Obtain corresponding salt by adding with fumaric acid saturated ether and carbinol mixture (9: 1).23 milligrams of output (2%).Mp?193.5-202.0℃。
In-(3,4-two chloro-phenyl)-(8-methyl-8-aza-bicyclo [3.2.1] oct-3-yl)-methane amide fumarate
Be from above reaction mixture, to separate according to method 1.32 milligrams of output, (3%), Mp206.3 ℃.
(3,4-two chloro-phenyl) outward-(8-methyl-8-aza-bicyclo [3.2.1] oct-3-yl)-methane amide fumarate
Be from outside-(3,4-two chloro-phenyl)-(8-methyl-8-aza-bicyclo [3.2.1] oct-3-yl)-amine carries out formylation with dense formic acid and makes.Aftertreatment is carried out according to method 1.Mp150.5-153.0℃。

Claims (12)

1. 8-aza-bicyclo [3.2.1] Octane derivatives of formula I:
Figure C2004800155750002C1
Or any mixture of any its isomer or its isomer,
Or its pharmacy acceptable salt,
Wherein
R aRepresent hydrogen or alkyl;
This alkyl randomly independently is selected from following one or more substituting group and is replaced: halogen, trifluoromethyl, trifluoromethoxy, cyano group, hydroxyl, amino, nitro, alkoxyl group, cycloalkyloxy, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl;
X representative-O-;
R bRepresent aryl or heteroaryl;
This aryl or heteroaryl randomly independently are selected from following substituting group and replace by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, hydroxyl, amino, nitro, oxo, alkoxyl group, cycloalkyloxy, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl
Condition is that described compound is not:
4[(3-is outer)-8-methyl-8-aza-bicyclo [3.2.1] oct-3-yl oxygen base] phenol, or
In-3-butoxy-4-(N-methyl-8-azabicyclo [3.2.1] suffering-3-oxygen base)-1,2, the 5-thiadiazoles.
2. the compound of claim 1, or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt, wherein R aRepresent hydrogen.
3. the compound of claim 1, or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt, wherein R aRepresent methylidene.
4. each compound of claim 1-3, or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt, wherein
R bRepresent aryl or heteroaryl;
This aryl or heteroaryl independently are selected from following substituting group and replace by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, oxo, alkyl and alkoxyl group.
5. each compound of claim 1-3, or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt, wherein R bRepresent phenyl,
This phenyl randomly independently is selected from following substituting group and replaces by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group and alkoxyl group.
6. each compound of claim 1-3, or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt, wherein R bRepresent thienyl,
This thienyl independently is selected from following substituting group and replaces by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group and alkoxyl group.
7. each compound of claim 1-3, or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt, wherein R bRepresent pyridyl,
This pyridyl independently is selected from following substituting group and replaces by one or more: halogen, trifluoromethyl, trifluoromethoxy, cyano group, hydroxyl and alkoxyl group.
8. the compound of claim 1, or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt, it is
In-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(3,4-dichloro-thiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(1,2-benzisothiazole-3-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-bromo thiazole-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(benzisothiazole-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-chloro benzothiazole-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoxaline-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(benzoxazol-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-chloro-pyridazine-3-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-chloro-pyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(isoquinolyl-1 oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-chloropyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-bromopyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-bromopyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-bromo pyrimi piperidine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(quinazoline-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-5-flumethiazine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4,5-three bromothiophenes-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-bromothiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(3-bromo-5-chloro-thiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(4-bromo-5-chloro-thiophene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2, the 3-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4,5-three chlorothiophenes-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-4-fluorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-fluorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2-ammonia-3-trifluoromethyl-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(fluorenes-9-ketone-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(1,2-benzisothiazole-3-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
In-3-(3, the 4-dichlorophenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-4-trifluoromethylphenopendant)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2-diphenylene-oxide oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(1-naphthyloxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2-naphthyloxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-4-cyanogen phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-methylphenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloronaphthalene-1-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(5-chloro-pyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methoxyl group phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(isoquinoline 99.9-5-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-bromo-naphthalene-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-bromo-3-chloro-phenoxy group)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-6-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-trifluoromethoxy phenoxy base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-cyano-benzene oxygen)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-8-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methylphenoxy)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-chloropyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(5-bromopyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-bromopyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(isoquinolyl-1 oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(3-Trifluoromethyl phenyl ether oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-Trifluoromethyl phenyl ether oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-methoxypyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(5-5-flumethiazine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(6-ethoxy pyridine-2-base oxygen base)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(4-fluoro-3-4-trifluoromethylphenopendant)-8-H-8-azabicyclo [3.2.1] octane;
Outward-3-(2, the 3-dichlorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-4-fluorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-fluorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(2-chloro-3-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(fluorenes-9-ketone-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(1-naphthyloxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(2-naphthyloxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-chloro-4-cyano-benzene oxygen)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(2-diphenylene-oxide oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloronaphthalene-1-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-chloro-3-methylphenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methoxyl group phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(7-methoxynaphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-methoxynaphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-bromo-3-chloro-phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(isoquinoline 99.9-5-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-bromo-naphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-methoxyl group phenoxy group)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-cyano-benzene oxygen)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(quinoline-6-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(1,2,3,4-naphthane-6-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methylphenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(8-quinolyl oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(5-indanyl oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-methoxynaphthalene-1-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(indoles-5-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3-Trifluoromethyl phenyl ether oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-Trifluoromethyl phenyl ether oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(4-fluoro-3-4-trifluoromethylphenopendant)-8-methyl-8-azabicyclo [3.2.1] octane;
In-3-(3, the 4-dichlorophenoxy)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(3,4-diamino phenoxy group)-8-(2-hydroxyethyl)-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-(cyano methyl)-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-(cyclopropyl methyl)-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-(allyl group)-8-azabicyclo [3.2.1] octane;
Outward-3-(3, the 4-dichlorophenoxy)-8-(methoxy ethyl)-8-azabicyclo [3.2.1] octane;
Outward-3-(6-methoxypyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-ethoxy pyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-hydroxyl-pyridine-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Outward-3-(6-cyano group-naphthalene-2-base oxygen base)-8-methyl-8-azabicyclo [3.2.1] octane;
Or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt.
9. pharmaceutical composition, it comprises each the compound of claim 1-8 for the treatment of significant quantity, or any mixture of any its isomer or its isomer, or its pharmacy acceptable salt class, and at least a pharmaceutically acceptable carrier, vehicle or thinner.
10. each compound or any mixture of any its isomer or its isomer or the purposes that its pharmacy acceptable salt is used to prepare medicine of claim 1-8.
11. the purposes of claim 10 is used to prepare treatment, prevent or alleviate the pharmaceutical composition of mammiferous disease or obstacle or illness, described disease, obstacle or illness are replied the inhibition of the monoamine neurotransmitter re-uptake in the central nervous system.
12. the purposes of claim 11, wherein said disease, obstacle or illness are emotional handicap, depressed, the evil mood obstacle, bipolar disorder, the cyclothymia obstacle, pseudodementia, Ganser's syndrome, obsessional idea and behavior disorder, Phobias, the agoraphobia of no Phobias medical history, panic attack, memory impairment, the loss of memory, attention deficit hyperactivity disease, fat, anxiety, eating disorder, Parkinson's disease, Parkinson, dull-witted, Alzheimer, the dull-witted complex of acquired immune deficiency syndrome (AIDS), aging memory machine dysfunction, specific phobia disease, social phobia, nervous obstacle after the wound, acute nervous obstacle, drug habit, drug abuse, cocaine abuse, the nicotine abuse, tobacco abuse, alcohol addiction, alcoholism, pain, fibromyalgia, sacroiliitis, irritable bowel syndrome, drug-induced neuropathy, diabetic neuropathy, exessive appetite, syndrome before the menstruation, the evening luteal phase syndrome, posttraumatic syndrome, chronic fatigue syndrome, the urinary incontinence, sexual dysfunction, eating disorder, anorexia nervosa, somnopathy, autism, mutism, trichotillomania, hypnolepsy, the apoplexy retarded depression, apoplexy inductive brain injury, apoplexy inductive neuronal damage or Du Leite disease.
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